rs796052799

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs796052799(C;G)

Make rs796052799(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408161

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052799
dbSNP (classic)	rs796052799
ClinGen	rs796052799
ebi	rs796052799
HLI	rs796052799
Exac	rs796052799
Gnomad	rs796052799
Varsome	rs796052799
LitVar	rs796052799
Map	rs796052799
PheGenI	rs796052799
Biobank	rs796052799
1000 genomes	rs796052799
hgdp	rs796052799
ensembl	rs796052799
geneview	rs796052799
scholar	rs796052799
google	rs796052799
pharmgkb	rs796052799
gwascentral	rs796052799
openSNP	rs796052799
23andMe	rs796052799
SNPshot	rs796052799
SNPdbe	rs796052799
MSV3d	rs796052799
GWAS Ctlg	rs796052799

Max Magnitude

0

ClinVar
Risk	rs796052799(G;G)
Alt	rs796052799(G;G)
Reference	Rs796052799(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663159G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000188349.2,